RecruitingAplastic AnemiaCytopeniaHypocellular Marrow
A Study of Emapalumab for Pediatric Aplastic Anemia
Eligible age
0–25 yrs
Accepts
All genders
Locations
5 states
Healthy volunteers
Yes
See if you qualify for this study
Answer a few quick questions about your location and health. Takes about a minute.
About this study
The purpose of this study is to find out whether upfront emapalumab treatment can help in sAA (Aplastic Anemia) treatment planning and increase the effectiveness of standard treatment options. Funding Source- FDA OOPD
Sponsor: Memorial Sloan Kettering Cancer Center
You may qualify if…
- ✓ Patients undergoing workup for suspected newly diagnosed sAA:
- ✓ Patients with severe cytopenias and a hypocellular marrow concerning for sAA
- ✓ Patients that meet the definition for suspected sAA (Camitta Criteria) as follows:
- ✓ Marrow Cellularity: \<25%, or 25-50% with \<30% residual hematopoietic cells Peripheral cytopenias (at least 2 of 3) Absolute neutrophil count (ANC): \<500 x 10\^9/L Platelets: \<20 x 10\^9/L Absolute Reticulocyte Count: \<60 x 10\^9/L
- ✓ Patients that do not have evidence of leukemia or MDS
- ✓ Patients \< 25 years of age at time of diagnosis
- ✓ Able to tolerate emapalumab and IST (with standard institutional organ function criteria)
You may not qualify if…
- ✕ Uncontrolled infection at presentation.
- ✕ Patients who have undergone previous treatment for sAA.
- ✕ Patients with known inherited bone marrow failure
- ✕ Patient who has completed a full workup for sAA including having results back from telomere testing, DEB and genetics (when applicable), as well as having an appropriate willing and available donor and would otherwise be admitted for HSCT within 2 weeks of enrolling on the trial
- ✕ Patients with leukemia or MDS
- ✕ Patient or parent or guardian unable to give informed consent or unable to comply with the treatment protocol including research tests.
Where it's recruiting
Source: ClinicalTrials.gov · NCT06430788 · last updated 2025-12-17